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p-Bromoacetophenone → 2-(4-Bromophenyl)quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Bromoacetophenone | HCID 7466 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 2-Aminobenzophenone | HCID 76080 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4-Bromophenyl)quinoline | HCID 1473444 | 78.3% |
反応手順
Dissolving 5.0 g (25 mmol) of 4-bromoacetophenone and 5.0 g (25 mmol) of 2-aminobenzophenon into 50 milliliter of ethanol, adding 3.1 g of sodium hydroxide, the resultant suspension was refluxed under heating for 7 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and ethanol, thereby obtaining 5.56 g of 2-(4-bromo-phenyl)-quinoline (yield: 61%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07867629B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-c554a8b419c44fce967ba6f31283fd67 |
| 出典メモ | uspto-grants-2011_01 |